| alphafold_model | The predicted structure for a UniProt accession |
| alphafold_parse_model | Turn an AlphaFold prediction response into a table |
| civic_gene | Curated clinical evidence counts for a gene |
| civic_parse_gene | Turn a CIViC gene response into a table |
| clingen_alleles | Resolve HGVS to canonical allele ids |
| clingen_gene_validity | The ClinGen gene-disease validity table |
| clingen_parse_allele | Turn one Allele Registry element into a table row |
| clingen_parse_batch | Turn an Allele Registry batch response into a table |
| clingen_parse_validity | Parse the ClinGen gene-validity CSV |
| clingen_validity_for | Filter a parsed validity table to one or more genes |
| clinvar_category | Bucket a ClinVar significance string into a coarse category |
| clinvar_classification | Look up the ClinVar classification for a variant |
| clinvar_conditions | Collapse a ClinVar trait set into one condition string |
| clinvar_parse_record | Turn a ClinVar esummary record into a table |
| dgidb_gene | Drug-gene interaction count for one gene |
| dgidb_genes | Drug-gene interaction counts for many genes |
| dgidb_parse_genes | Turn a DGIdb genes response into a table |
| diseases_channel | Genes DISEASES associates with a disease, from one channel |
| diseases_gene_associations | Genes DISEASES associates with a disease, across both channels |
| diseases_merge_channels | Combine DISEASES channels, keeping the strongest score per gene |
| diseases_parse_channel | Turn one DISEASES channel response into a table |
| ensembl_gene_model | The exon model for a gene |
| ensembl_parse_consequences | Turn Ensembl transcript consequences into a table |
| ensembl_parse_gene_model | Turn an Ensembl gene lookup into a gene model |
| ensembl_parse_vep | Turn an Ensembl VEP record into a result |
| ensembl_vep_id | Run VEP for a variant id |
| europepmc_count | How many publications Europe PMC has for a query |
| europepmc_parse_count | Read the hit count off a Europe PMC response |
| europepmc_parse_results | Turn Europe PMC search results into a table |
| europepmc_query | Build a Europe PMC query from terms |
| europepmc_search | Search Europe PMC |
| gnomad_constraint | Gene constraint for one gene |
| gnomad_constraints | Gene constraint for many genes |
| gnomad_frequencies | Population allele frequency for many variants |
| gnomad_frequency | Population allele frequency for a variant |
| gnomad_frequency_by_id | Population allele frequency for a variant, by id |
| gnomad_parse_constraint | Turn a gnomAD constraint response into a table |
| gnomad_parse_constraints | Turn an aliased gnomAD constraint response into a table |
| gnomad_parse_frequency | Turn a gnomAD variant response into a frequency record |
| gnomad_parse_populations | Combine gnomAD per-ancestry counts into one frequency table |
| gnomad_parse_variant | Turn a gnomAD variant response into a frequency row |
| gnomad_parse_variants | Turn an aliased gnomAD variant response into a table |
| gnomad_variant_id | Build a gnomAD variant id from variant components |
| gtex_gene_reference | Resolve a gene to GTEx's versioned GENCODE id |
| gtex_median_expression | Median expression across tissues |
| gtex_parse_expression | Turn a GTEx median-expression response into a table |
| gtex_parse_reference | Turn a GTEx gene-reference response into a table |
| hpa_gene | The Human Protein Atlas record for a gene |
| hpa_parse_gene | Turn an HPA gene record into a table |
| hpo_gene_annotation | HPO's annotation for a gene |
| hpo_parse_diseases | Turn an HPO gene annotation into a table of diseases |
| hpo_parse_phenotypes | Turn an HPO gene annotation into a table of phenotypes |
| hpo_parse_search | Turn an HPO search response into a table |
| hpo_parse_term | Turn an HPO term response into a table |
| hpo_search | Search HPO terms by free text |
| hpo_term | Resolve one HP id to its term |
| impc_gene_phenotypes | Significant knockout phenotypes IMPC records for a human gene |
| impc_mouse_ortholog | The mouse ortholog IMPC holds for a human gene |
| impc_parse_ortholog | Read the mouse ortholog out of an IMPC gene-core response |
| impc_parse_phenotypes | Turn an IMPC phenotype response into a table |
| monarch_associations | Associations with an entity on one end |
| monarch_gene_phenotypes | HPO phenotypes Monarch associates with a gene |
| monarch_hgnc_id | Normalise an HGNC id to the CURIE form Monarch expects |
| monarch_parse_associations | Turn Monarch association records into a table |
| monarch_parse_search | Turn a Monarch search response into a table |
| monarch_search | Search Monarch for an entity |
| mygene_gene | Look up one gene |
| mygene_genes | Look up many genes in one request |
| mygene_parse_batch | Turn a MyGene batch response into a gene table |
| mygene_parse_hits | Turn MyGene hits into a gene table |
| mygene_pick_hit | Choose the best MyGene hit for a queried token |
| myvariant_id | Build a MyVariant identifier from variant components |
| myvariant_parse_batch | Turn a MyVariant batch response into a table |
| myvariant_parse_record | Turn one MyVariant record into a table row |
| myvariant_variants | Annotate many variants in one request |
| opentargets_disease_targets | Genes associated with a disease |
| opentargets_drugs | Known drugs and clinical candidates for a gene |
| opentargets_gene_diseases | Diseases associated with a gene |
| opentargets_is_id | Is a term an ontology id rather than free text |
| opentargets_parse_diseases | Turn target-to-disease rows into a table |
| opentargets_parse_drugs | Turn known-drug rows into a table |
| opentargets_parse_matches | Turn a disease search or lookup into a table |
| opentargets_parse_pgx | Turn pharmacogenomics rows into a table |
| opentargets_parse_targets | Turn disease-to-target rows into a table |
| opentargets_pgx | Pharmacogenomics annotations for a gene |
| opentargets_resolve_disease | Resolve a disease term to ontology records |
| panelapp_all_panels | The whole PanelApp panel index |
| panelapp_panel | The genes on one PanelApp panel |
| panelapp_panels | One page of the PanelApp panel index |
| panelapp_parse_index | Turn a PanelApp panel index page into a table |
| panelapp_parse_panel | Turn a PanelApp panel detail into a table of genes |
| pdbe_parse_structures | Turn a PDBe best-structures response into a table |
| pdbe_structures | Experimental structures for a UniProt accession |
| pharos_parse_targets | Turn a Pharos targets response into a table |
| pharos_target | Target Development Level for one gene |
| pharos_targets | Target Development Level for many genes |
| protvar_function | Functional context for a residue |
| protvar_parse_function | Turn a ProtVar function response into its text |
| protvar_parse_population | Turn a ProtVar population response into a table |
| protvar_population | Known variants at a residue |
| protvar_position | Pull a residue position out of a protein-change string |
| protvar_strip_citations | Strip inline citations out of a UniProt function comment |
| pubtator_entity | Build the PubTator3 entity token for a gene |
| pubtator_gene_literature | Articles PubTator3 has tagged with a gene |
| pubtator_parse_count | Read the article count off a PubTator3 search response |
| pubtator_parse_results | Turn PubTator3 search results into a table |
| quickgo_annotations | GO annotations for a UniProt accession |
| quickgo_parse_annotations | Turn a QuickGO annotation response into a table |
| reactome_parse_pathways | Turn a Reactome pathway array into a table |
| reactome_pathways | Reactome pathways for a gene symbol |
| string_map_ids | The STRING identifier map for a set of symbols |
| string_network | The interaction network within a set of genes |
| string_parse_ids | Turn a STRING identifier-map response into a table |
| string_parse_network | Turn a STRING network response into an edge table |
| string_parse_partners | Turn STRING interaction-partner rows into a table |
| string_partners | Interaction partners for one gene |
| string_reconcile_edges | Rewrite edge endpoints back into the queried symbol space |
| uniprot_diseases | Diseases UniProt curates for an accession |
| uniprot_features | Sequence features for an accession |
| uniprot_features_at | The features spanning a residue position |
| uniprot_parse_diseases | Turn a UniProtKB entry into a curated-disease table |
| uniprot_parse_features | Turn an EBI Proteins features response into a table |
| variantvalidator_normalize | Validate and normalize one HGVS variant |
| variantvalidator_parse | Turn a VariantValidator response into a table |
| vep_default_options | The request flags VEP is asked for by default |
| vep_default_throttle | The default rate limit for VEP requests |
| vep_key | Build the variant key VEP results are matched on |
| vep_parse_batch | Turn a VEP batch response into a table |
| vep_parse_colocated | Turn the colocated variants of a VEP element into a table row |
| vep_parse_element | Turn one VEP element into a table row |
| vep_pick_transcript | Choose which transcript to report for a variant |
| vep_region | Build a VEP region string from variant components |
| vep_variants | Consequence predictions for many variants |
| vep_variants_all | Consequence predictions for any number of variants |